Ozaki N, Nakahara D, Kaneda N, Kiuchi K, Okada T, Kasahara Y, Nagatsu T
Department of Psychiatry, Nagoya University School of Medicine, Japan.
J Neural Transm. 1987;70(3-4):241-50. doi: 10.1007/BF01253601.
The acute effect of 1-methyl-4-phenylpyridinium ion (MPP+), a neurotoxin derived from 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), was examined by the in vivo micro-dialysis technique. A dialysis cannula was implanted into rat striatum, and the changes in the concentrations of dopamine (DA), 3, 4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA), and 5-hydroxyindoleacetic acid (5-HIAA) in the perfusate every 20 min after administration of MPP+ were determined by high-performance liquid chromatography with electrochemical detection (HPLC-ED). After MPP+ administration the levels of DOPAC, HVA and 5-HIAA were markedly decreased. On the contrary the level of DA was markedly increased and reached a maximum 40 min after beginning of the MPP+ administration. By postmortem analysis of the striatal tissue MPP+ was proved to cause the inhibition of monoamine oxidase (MAO), especially MAO-B. These results suggest that the acute biochemical changes induced by MPP+ in vivo were MAO inhibition and release of DA.
采用体内微透析技术研究了1-甲基-4-苯基吡啶离子(MPP+)(一种由1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)衍生而来的神经毒素)的急性效应。将透析套管植入大鼠纹状体,通过高效液相色谱-电化学检测法(HPLC-ED)测定给予MPP+后每隔20分钟灌流液中多巴胺(DA)、3,4-二羟基苯乙酸(DOPAC)、高香草酸(HVA)以及5-羟吲哚乙酸(5-HIAA)浓度的变化。给予MPP+后,DOPAC, HVA和5-HIAA的水平显著降低。相反,DA水平显著升高,并在开始给予MPP+后40分钟达到最大值。通过对纹状体组织的死后分析,证实MPP+可导致单胺氧化酶(MAO)尤其是MAO-B的抑制。这些结果表明,MPP+在体内诱导的急性生化变化是MAO抑制和DA释放。